1030385-16-0 Usage
Description
(S)-2-benzylamino-1-((R)-6-fluoro-3,4-dihydro-2H-chromen-2-yl)ethanol is a chiral chemical compound with the molecular formula C20H22FNO2. It features a benzylamino group, a fluoro substituent, and a chromen-2-yl moiety, which contribute to its potential pharmacological properties. (S)-2-benzylamino-1-((R)-6-fluoro-3,4-dihydro-2H-chromen-2-yl)ethanol is significant in the field of medicinal chemistry, where it may be utilized in the development of new drugs or serve as a research tool.
Uses
Used in Pharmaceutical Industry:
(S)-2-benzylamino-1-((R)-6-fluoro-3,4-dihydro-2H-chromen-2-yl)ethanol is used as a potential drug candidate for the development of new pharmaceuticals due to its unique structural features and chiral nature. Its synthesis and characterization can provide valuable insights for scientists studying its potential applications in treating various medical conditions.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (S)-2-benzylamino-1-((R)-6-fluoro-3,4-dihydro-2H-chromen-2-yl)ethanol is used as a research tool to explore its pharmacological properties and understand its interactions with biological targets. This knowledge can contribute to the advancement of drug discovery and the development of novel therapeutic agents.
Used in Drug Synthesis:
(S)-2-benzylamino-1-((R)-6-fluoro-3,4-dihydro-2H-chromen-2-yl)ethanol can be employed as a key intermediate in the synthesis of more complex drug molecules. Its unique structural elements may enable the creation of new compounds with improved pharmacological profiles and therapeutic potential.
Used in Drug Design:
As a chiral molecule with distinct functional groups, (S)-2-benzylamino-1-((R)-6-fluoro-3,4-dihydro-2H-chromen-2-yl)ethanol can be utilized in drug design to create enantiomerically pure compounds with specific biological activities. This can lead to the development of more effective and safer medications with fewer side effects.
Check Digit Verification of cas no
The CAS Registry Mumber 1030385-16-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,0,3,8 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1030385-16:
(9*1)+(8*0)+(7*3)+(6*0)+(5*3)+(4*8)+(3*5)+(2*1)+(1*6)=100
100 % 10 = 0
So 1030385-16-0 is a valid CAS Registry Number.
1030385-16-0Relevant articles and documents
Synthesis of intermediate compound and [...] (by machine translation)
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Paragraph 0242-0243; 0275-0277, (2020/04/09)
Synthesis of intermediate compounds [a] and [...]. [Solution] a [...], asymmetric epoxidation, sulfonyl halide in the presence of base catalyst by sulfonation, alkylation of amines, such as synthesized by a series of cross-coupling reaction. [Effect] [...] important from the viewpoint of pharmacological value, high efficiency, low cost, and which meets the requirements of industrial, optical isomers may be prepared [...] and develop a method, which is very economical in social benefit. [Drawing] no (by machine translation)
Nebivolol synthetic method and intermediate compounds of the
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Paragraph 0418; 0420; 0490-0492, (2018/10/04)
The present invention relates to a synthesis method and an intermediate compound of nebivolol. Specifically the invention relates to the method for synthesizing the nebivolol, the intermediate compound of the nebivolol, and a method for preparing the intermediate compound.
A NEW METHOD FOR PRODUCING NEBIVOLOL HYDROCHLORIDE OF HIGH PURITY
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, (2015/09/22)
The invention relates to a process for producing Nebivolol hydrochloride, (formula I) comprising the steps of: provision of a protected Nebivolol hydrochloride of the general formula (II), with P being an amine protecting group, and hydrogenation of said protected Nebivolol hydrochloride yielding Nebivolol hydrochloride of the formula (I).
